rs786203845
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 6 | BRCA2 variant considered pathogenic for breast cancer |
Make rs786203845(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 32336315 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs786203845 |
dbSNP (classic) | rs786203845 |
ClinGen | rs786203845 |
ebi | rs786203845 |
HLI | rs786203845 |
Exac | rs786203845 |
Gnomad | rs786203845 |
Varsome | rs786203845 |
LitVar | rs786203845 |
Map | rs786203845 |
PheGenI | rs786203845 |
Biobank | rs786203845 |
1000 genomes | rs786203845 |
hgdp | rs786203845 |
ensembl | rs786203845 |
geneview | rs786203845 |
scholar | rs786203845 |
rs786203845 | |
pharmgkb | rs786203845 |
gwascentral | rs786203845 |
openSNP | rs786203845 |
23andMe | rs786203845 |
SNPshot | rs786203845 |
SNPdbe | rs786203845 |
MSV3d | rs786203845 |
GWAS Ctlg | rs786203845 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786203845(T;T) |
Alt | rs786203845(T;T) |
Reference | Rs786203845(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Breast-ovarian cancer |
Variation | info |
Gene | BRCA2 |
CLNDBN | Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.32910452G>T |
CLNSRC | |
CLNACC | RCV000167330.1, RCV000241155.1, |